diff --git a/src/contents/methods.tsx b/src/contents/methods.tsx
index 7d947d138078c2177c2442c9f72481ef7bf8d9d7..30e1503b2e814f5e9bb07966d6d69852fbbfefc7 100644
--- a/src/contents/methods.tsx
+++ b/src/contents/methods.tsx
@@ -91,7 +91,7 @@ export function Methods() {
             <p>In addition to assessing immediate cytotoxicity, we also evaluated the long-term safety of the LNPs by conducting a proliferation assay. This assay tracked cell division and growth over time to determine whether the LNPs impacted cellular function. Our results showed that LNP-treated cells had similar growth rates to untreated controls, indicating that the LNPs do not interfere with normal cell processes. This further confirms their biocompatibility and suitability for use in biological systems.</p>
           </Subesction>
           <Subesction title="Flow cytometry" id="flow cytometry">
-            <p>To assess the transfection efficiency of our LNPs, we used flow cytometry. This method involved tagging the LNPs with fluorescent markers and measuring their ability to deliver genetic material into target cells. FACS provided quantitative insights into how effectively the LNPs transfected cells, helping us optimize their design for gene therapy applications. </p>
+            <p>To assess the transfection efficiency of our LNPs, we used flow cytometry. This method involved tagging the LNPs with fluorescent markers and measuring their ability to deliver genetic material into target cells. The flow cytometry provided quantitative insights into how effectively the LNPs transfected cells, helping us optimize their design for gene therapy applications. </p>
           </Subesction>
 
           <Subesction title="In-Depth Characterization of LNPs" id="In-Depth Characterization of LNPs">